Efforts to Increase Representation in Prostate Cancer Clinical Trials at Lyndon B. Johnson Hospital

Clinicaltrials.gov ID: NCT07591701
db-list-check Status RECRUITING
b-loader Phase NA
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 60

Conditions

Prostate Cancer

Summary

The main rationale underlying this study is that prostate cancer clinical trials are lacking representation from racial and ethnic minority groups. Study proposal aims to target barriers at the participant, investigator, and health system level through specific interventions to increase the percentage of participants from these backgrounds on cancer clinical trials.

Detailed Description

Primary Objectives:

The study objective is to increase the number of participants on prostate cancer clinical trials at LBJ. Investigators will complete several objectives:

* To design a culturally tailored video highlighting participant narratives and determine its impact on participants’ decision-making pertaining to joining a clinical trial
* To conduct educational sessions with frontline oncology providers
* To coordinate participant care through utilization of a nurse navigator
* To evaluate the effectiveness of this multi-pronged intervention to increase enrollment onto two prostate cancer clinical trials and compare enrollment and one-year retention rates before and after the intervention

Locations

1 location Found with status Recruiting

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Debanjan Pain, MD

Eligibility Criteria

Inclusion Criteria:

These criteria include diagnosed prostate cancer patients receiving care at LBJ Hospital who

Are eligible for an open prostate cancer clinical trial at LBJ Hospital during the study period

Can provide informed consent.

Exclusion Criteria:

These criteria include prostate cancer patients receiving care at LBJ who are unable to participate due to a serious psychological or cognitive condition or have a medical condition that prevents participation in the trial.

Outcome Measures

Primary Outcome Measures

Safety and Adverse Events (AEs)

Time Frame: Through study completion; an average of 1 year

Timeline

  • Last Updated
    June 26, 2026
  • Start Date
    May 18, 2026
  • Today
    October 1, 2026
  • Completion Date ( Estimated )
    January 31, 2030

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